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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654355Generated: October 29, 2026

Pyridine → HCID 57029440, compound

https://huagongshe.com/reaction/654355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTert-ButylamineHCID 6385—
ReactantOxalyl chlorideHCID 65578—
Reactant5327-60-6HCID 220506—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 57029440HCID 57029440—

Reaction Steps

A stirred suspension of 3-oxopregn-4-ene-20-carboxylic acid (1.7 g, 5.0 mmole) in benzene (35 mL) was mixed with pyridine (0.56 mL, 6.25 mmole), cooled in an ice-water bath and treated with oxalyl chloride (0.56 mL, 6.45 mmole). The cooling bath was removed and the reaction mixture was stirred for 1.5 hours. The resulting mixture was then cooled in ice and treated slowly with tert-butylamine (2.9 mL, 29 mmole). After thirty minutes, the mixture was diluted with methylene chloride (100 mL), extracted with 5% hydrochloric acid, dried over magnesium sulfate, treated with charcoal, and filtered. The resulting filtrate was concentrated to give a yellow solid which was dissolved in methylene chloride and purified by flash chromatography (hexane-40% ethyl acetate). The product obtained in this way was subjected to flash chromatography again (hexane-30% ethyl acetate) and the resulting product was recrystallized from acetone to give (20S)-N-(1,1-dimethylethyl)-3-oxopregn-4-ene-20-carboxamide. IR 3445, 3375, 1670 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05130424
Source datasetuspto-grants-1992_07
ORD IDord-093e2c53e5a34d9fb5ac506b09c4c953
Source noteuspto-grants-1992_07